Estriol succinate

• CAT Number: I027029
• CAS Number: 514-68-1
• Molecular Formula: C26H32O9
• Molecular Weight: 488.53
• Purity: 98%
• Synonyms: Estriol succinate; Estrioli succinas; Oestriol succinate
• Solubility: To be determined
• Appearance: Solid powder
• Storage: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
• IUPAC Name: 4,4'-(((8R,9S,13S,14S,16R,17R)-3-hydroxy-13-methyl-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthrene-16,17-diyl)bis(oxy))bis(4-oxobutanoic acid)
• InChI: InChI=1S/C26H32O9/c1-26-11-10-17-16-5-3-15(27)12-14(16)2-4-18(17)19(26)13-20(34-23(32)8-6-21(28)29)25(26)35-24(33)9-7-22(30)31/h3,5,12,17-20,25,27H,2,4,6-11,13H2,1H3,(H,28,29)(H,30,31)/t17-,18-,19+,20-,25+,26+/m1/s1
• InChIKey: VBRVDDFOBZNCPF-BRSFZVHSSA-N
• SMILES: C[C@]12CC[C@H]3[C@H]([C@@H]1C[C@H]([C@@H]2OC(=O)CCC(=O)O)OC(=O)CCC(=O)O)CCC4=C3C=CC(=C4)O

Estriol Succinate(CAT: I027029) is a synthetic derivative of estriol, a naturally occurring estrogen, widely utilized in pharmaceutical and biochemical research. This compound serves as a key tool for studying estrogen receptor signaling pathways, hormone replacement therapies, and reproductive health. Its stable and bioactive profile makes it suitable for investigating estrogen’s role in cellular growth, differentiation, and metabolic regulation. Estriol Succinate is ideal for in vitro and in vivo studies, providing researchers with reliable insights into hormonal mechanisms and aiding in the development of novel therapeutic approaches targeting estrogen-related conditions.